Manufacturer registered with FDA

Selenium Medical S.A.S.

La Rochelle, France. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10045214Contract manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
21 registrations outside the US
Establishments
1France

Registered in 2 markets

Where regulators' registries name Selenium Medical S.A.S. as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedBrazil: 1 registrations
RegisteredHome: FranceOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSelenium Medical S.A.S.2 device types—Below
BrazilANVISARegistration holderSELENIUM MEDICAL LTDA12023–2023Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Selenium Medical S.A.S. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker
KONTACT DENTAL IMPLANT SYSTEM
2021
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
KONTACT DENTAL IMPLANT SYSTEM
2021

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Registered establishments

EstablishmentLocationWhat it does
SELENIUM MEDICAL S.A.S.FDA reg. 1000461041La Rochelle Charente-Maritime, FranceContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10045214). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.